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16 pages, 5164 KiB  
Article
Effects of the Interaction between Rumen Microbiota Density–VFAs–Hepatic Gluconeogenesis on the Adaptability of Tibetan Sheep to Plateau
by Wenxin Yang, Yuzhu Sha, Xiaowei Chen, Xiu Liu, Fanxiong Wang, Jiqing Wang, Pengyang Shao, Qianling Chen, Min Gao and Wei Huang
Int. J. Mol. Sci. 2024, 25(12), 6726; https://doi.org/10.3390/ijms25126726 - 19 Jun 2024
Viewed by 958
Abstract
During the adaptive evolution of animals, the host and its gut microbiota co-adapt to different elevations. Currently, there are few reports on the rumen microbiota–hepato-intestinal axis of Tibetan sheep at different altitudes. Therefore, the purpose of this study was to explore the regulatory [...] Read more.
During the adaptive evolution of animals, the host and its gut microbiota co-adapt to different elevations. Currently, there are few reports on the rumen microbiota–hepato-intestinal axis of Tibetan sheep at different altitudes. Therefore, the purpose of this study was to explore the regulatory effect of rumen microorganism–volatile fatty acids (VFAs)–VFAs transporter gene interactions on the key enzymes and genes related to gluconeogenesis in Tibetan sheep. The rumen fermentation parameters, rumen microbial densities, liver gluconeogenesis activity and related genes were determined and analyzed using gas chromatography, RT-qPCR and other research methods. Correlation analysis revealed a reciprocal relationship among rumen microflora–VFAs-hepatic gluconeogenesis in Tibetan sheep at different altitudes. Among the microbiota, Ruminococcus flavefaciens (R. flavefaciens), Ruminococcus albus (R. albus), Fibrobactersuccinogenes and Ruminobacter amylophilus (R. amylophilus) were significantly correlated with propionic acid (p < 0.05), while propionic acid was significantly correlated with the transport genes monocarboxylate transporter 4 (MCT4) and anion exchanger 2 (AE2) (p < 0.05). Propionic acid was significantly correlated with key enzymes such as pyruvate carboxylase, phosphoenolpyruvic acid carboxylase and glucose (Glu) in the gluconeogenesis pathway (p < 0.05). Additionally, the expressions of these genes were significantly correlated with those of the related genes, namely, forkhead box protein O1 (FOXO1) and mitochondrial phosphoenolpyruvate carboxykinase 2 (PCK2) (p < 0.05). The results showed that rumen microbiota densities differed at different altitudes, and the metabolically produced VFA contents differed, which led to adaptive changes in the key enzyme activities of gluconeogenesis and the expressions of related genes. Full article
(This article belongs to the Section Molecular Microbiology)
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Figure 1
<p>Rumen microbiota densities at different altitudes. Note: *** indicates a highly significant difference (<span class="html-italic">p</span> &lt; 0.001); ns indicates that the difference is not significant.</p>
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<p>Expression of rumen epithelial transporter genes at different altitudes. Note: *** indicates a highly significant difference (<span class="html-italic">p</span> &lt; 0.001); * Indicates a significant difference (<span class="html-italic">p</span> &lt; 0.05); ns indicates that the difference is not significant.</p>
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<p>Liver gluconeogenesis key enzyme content and glucose content in Tibetan sheep at different altitudes: (<b>a</b>) Liver key enzyme content at different altitudes; (<b>b</b>) liver glucose content at different altitudes. Note: *** indicates a highly significant difference (<span class="html-italic">p</span> &lt; 0.001); ** indicates a highly significant difference (<span class="html-italic">p</span> &lt; 0.01); ns indicates a non-significant difference.</p>
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<p>Expressions of liver gluconeogenesis-related genes at different altitudes. Note: *** indicates a highly significant difference (<span class="html-italic">p</span> &lt; 0.001); * indicates a significant difference (<span class="html-italic">p</span> &lt; 0.05); ns indicates that the difference is not significant.</p>
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<p>Rumen microbiota density–VFAs–VFAs transporter gene correlations heat map. Note: Correlation heatmap * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Heat map of rumen VFAs–hepatic gluconeogenesis function correlations. Note: Correlation heatmap * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>The interaction model of Tibetan sheep rumen microbiota density–VFAs–liver gluconeogenesis axis. Note: The bold black solid line with an arrow in the figure represents the mechanism path of the rumen microbiota density–VFAs–hepatic gluconeogenesis axis. In terms of expression, red fonts represent up-regulation, blue fonts represent down-regulation, and black fonts represent insignificant differences.</p>
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15 pages, 2485 KiB  
Article
Dual-Omics Approach Unveils Novel Perspective on the Quality Control of Genetically Engineered Exosomes
by Christopher Olson, Konstantin Ivanov, Darin Boyes, David Bengford, Joy Ku, Renceh Flojo, Pengyang Zhang and Biao Lu
Pharmaceutics 2024, 16(6), 824; https://doi.org/10.3390/pharmaceutics16060824 - 18 Jun 2024
Viewed by 945
Abstract
Exosomes, nanoscale vesicles derived from human cells, offer great promise for targeted drug delivery. However, their inherent diversity and genetic modifications present challenges in terms of ensuring quality in clinical use. To explore solutions, we employed advanced gene fusion and transfection techniques in [...] Read more.
Exosomes, nanoscale vesicles derived from human cells, offer great promise for targeted drug delivery. However, their inherent diversity and genetic modifications present challenges in terms of ensuring quality in clinical use. To explore solutions, we employed advanced gene fusion and transfection techniques in human 293T cells to generate two distinct sets of genetically engineered samples. We used dual-omics analysis, combining transcriptomics and proteomics, to comprehensively assess exosome quality by comparing with controls. Transcriptomic profiling showed increased levels of engineering scaffolds in the modified groups, confirming the success of genetic manipulation. Through transcriptomic analysis, we identified 15 RNA species, including 2008 miRNAs and 13,897 mRNAs, loaded onto exosomes, with no significant differences in miRNA or mRNA levels between the control and engineered exosomes. Proteomics analysis identified changes introduced through genetic engineering and over 1330 endogenous exosome-associated proteins, indicating the complex nature of the samples. Further pathway analysis showed enrichment in a small subset of cellular signaling pathways, aiding in our understanding of the potential biological impacts on recipient cells. Detection of over 100 cow proteins highlighted the effectiveness of LC-MS for identifying potential contaminants. Our findings establish a dual-omics framework for the quality control of engineered exosome products, facilitating their clinical translation and therapeutic applications in nanomedicine. Full article
(This article belongs to the Special Issue Advances in Nanocarriers for Drug Delivery and Targeting, 2nd Edition)
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Figure 1
<p>Production and characterization of genetically modified exosomes in cultured human 293T cells. Schematic representation of the production and isolation of exosomes (<b>A</b>), which are used for further characterization and dual-omics analysis (<b>B</b>). After initial characterization studies, engineered exosomes were divided into two cohorts, which were subjected to next-generation sequencing analysis of whole transcripts (transcriptomics) or liquid chromatography coupled with mass spectrometry analysis (LC-MS, proteomics).</p>
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<p>Construct schematics and scaffold expression. (<b>A</b>) Schematic representation of constructs containing exosome-targeting scaffolds (CD9, CD63, CD81, VSVG) and molecular modifiers (GFP, CD47, mNCAM, Transferrin). (<b>B</b>) Confocal image study confirms successful scaffold targeting to sites of exosomal biogenesis (the plasma membrane and endocytic compartments). 293T cells were transfected with fusion protein constructs including CD9-GFP, CD63-GFP, CD81-GFP, and VSVG-GFP. Fluorescence images were recorded 72 h after transfection. The transmitted light images (TLI) show the corresponding morphology of the imaged cells. The punctuated plasm membrane (indicated by arrowheads) and endocytic compartment (indicated by arrows) became apparent when the fluorescent images were merged with the blue nuclei stained with HOCHEST. Scale bar, 10 μm.</p>
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<p>Characterization of genetically modified exosomes and non-modified controls. (<b>A</b>) Exosome size and distribution determined via nanoparticle tracking analysis (NTA). NTA profiles of CD9–GFP-, CD63–GFP-, CD81–GFP-, and VSVG–GFP-modified exosomes isolated from 293T cells at Day 3 post-transfection, showing the particle size and distribution of the respective engineered exosomes and the non-engineered control. (<b>B</b>) Exosome marker analysis via antibody array. The immuno-slot assay was able to detect different levels of cellular proteins loaded onto exosomes. PC: positive control; NC: negative control. (<b>C</b>) Fluorescence confocal images of isolated, genetically engineered exosomes (CD9–GFP, CD63–GFP, CD81–GFP, and VSVG–GFP) and non-engineered controls. White arrows indicate GFP-positivity for engineered exosomes, where background GFP noise is shown in the control sample. Scale bar, 50 μm.</p>
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<p>NGS sequencing unveiled enhanced levels of engineering scaffolds and GFP as compared to controls. (<b>A</b>) Human genome mapping of NGS data reveals elevated levels of scaffold proteins in their associated samples, including CD9 (1.78×), CD63 (27.96×), and CD81 (64.32×). Additional analysis via Geneious Prime highlights elevated levels of VSVG (14.5×) in the VSVG-GFP transfected sample (<b>B</b>) and GFP (29.2×–38.8×) in CD9, CD63, and CD81 samples (<b>C</b>). LC-MS detected increased levels of expression for CD47 in CD47-GFP (67×) and CD47-tVSVG-GFP (20×), human Transferrin in hTransferrin-tVSVG-GFP (270×), and GFP in GFP-modified exosome samples (except mNCAM-tVSVG-GFP), but not in control exosomes. LC-MS was not able to detect murine NCAM proteins (<b>D</b>).</p>
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<p>NGS sequencing identifies fifteen RNA types and reveals differences between engineered and control samples in key RNA subtypes. (<b>A</b>) Transcriptomics analysis reveals the presence of fifteen RNA types present in varying quantities in control samples (<span class="html-italic">n</span> = 2). (<b>B</b>) Comparison between control (<span class="html-italic">n</span> = 2) and engineered (<span class="html-italic">n</span> = 4) samples highlights significant differences in relative abundance of RNA transcripts in some subtypes (*** indicates <span class="html-italic">p</span> ≤ 0.001). Error bars show the standard error of the mean (SEM).</p>
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<p>Global profile of transcript and protein cargos by dual-omics. (<b>A</b>) Cross-sample comparison of mRNAs (count ≥ 25) reveals a cohort of shared mRNAs (11,996) and minimal differences between control and engineered samples prepared under the same culture conditions (Control 1, CD9, CD63, CD81, VSVG). Control 2, prepared under different culture conditions, contains the most variation, with 4485 unique mRNAs. (<b>B</b>) Cross-sample comparison of miRNAs (count ≥ 25) highlights a group of shared miRNAs (511) and minor differences between Control 1 and CD9 (19) and VSVG (78) engineered samples. Control 2, prepared from different batches, retains the most variation, with 205 unique miRNAs. (<b>C</b>) Cross-sample comparison of LC-MS protein data shows shared proteins (<span class="html-italic">n</span> = 1338) in all samples and unique proteins (<span class="html-italic">n</span> = 23–148) in individual samples.</p>
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15 pages, 971 KiB  
Article
Non-Fragile Prescribed Performance Control of Robotic System without Function Approximation
by Jianjun Zhang, Pengyang Han, Zhonghua Wu, Bo Su, Jinxian Yang and Juan Shi
Electronics 2024, 13(8), 1417; https://doi.org/10.3390/electronics13081417 - 9 Apr 2024
Viewed by 739
Abstract
In order to address the fragility issues associated with the current prescribed performance control (PPC) strategy and ensure both transient and steady-state performance of the tracking error, a non-fragility prescribed performance control scheme is proposed. A non-fragile prescribed performance control method for robotic [...] Read more.
In order to address the fragility issues associated with the current prescribed performance control (PPC) strategy and ensure both transient and steady-state performance of the tracking error, a non-fragility prescribed performance control scheme is proposed. A non-fragile prescribed performance control method for robotic systems with model uncertainties and unknown disturbances is developed. This method not only addresses the inherent vulnerability defects of the existing prescribed performance control but also effectively reduces the computational complexity of the controller. Firstly, addressing the fragility issues of existing PPC, a new non-fragile prescribed performance control strategy is proposed. To address the fragile issue with the current PPC, the shift function is employed to handle the tracking error. Based on the non-fragile PPC mentioned above, a new prescribed performance controller is designed without the requirement for approximation or estimation. This effectively reduces the complexity of controller design. At last, the feasibility of achieving non-fragile prescribed performance is verified through stability analysis, and the superiority of the designed controller is confirmed through simulation comparisons. The results show that the designed controller effectively resolves the control singularity issue arising from the inherent limitations of the PPC. Full article
(This article belongs to the Special Issue The Application of Control Systems in Robots)
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<p>Tracking performance in case 1.</p>
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<p>Tracking errors and the prescribed bounds in case 1.</p>
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<p>Control input in case 1.</p>
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<p>Transform error <math display="inline"><semantics> <mrow> <mi>ε</mi> <mo>(</mo> <mi>t</mi> <mo>)</mo> </mrow> </semantics></math> in case 1.</p>
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<p>Position tracking error in case 2.</p>
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<p>Position tracking error in case 2.</p>
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<p>Control input in case 2.</p>
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15 pages, 11162 KiB  
Article
Supplementation with Astragalus Root Powder Promotes Rumen Microbiota Density and Metabolome Interactions in Lambs
by Pengyang Shao, Yuzhu Sha, Xiu Liu, Yanyu He, Fanxiong Wang, Jiang Hu, Jiqing Wang, Shaobin Li, Xiaowei Chen, Wenxin Yang, Qianling Chen and Min Gao
Animals 2024, 14(5), 788; https://doi.org/10.3390/ani14050788 - 2 Mar 2024
Cited by 1 | Viewed by 1736
Abstract
The gut microbiota is highly symbiotic with the host, and the microbiota and its metabolites are essential for regulating host health and physiological functions. Astragalus, as a feed additive, can improve animal immunity. However, the effects of Astragalus root powder on the [...] Read more.
The gut microbiota is highly symbiotic with the host, and the microbiota and its metabolites are essential for regulating host health and physiological functions. Astragalus, as a feed additive, can improve animal immunity. However, the effects of Astragalus root powder on the rumen microbiota and their metabolites in lambs are not apparent. In this study, thirty healthy Hu sheep lambs with similar body weights (17.42 ± 2.02 kg) were randomly selected for the feeding experiment. Lambs were fed diets supplemented with 0.3% Astragalus root powder, and the rumen microbiota density and metabolome were measured to determine the effects of Astragalus on the health of lambs in the rumen. The results showed that the relative abundance of Butyrivibrio fibrisolvens (Bf), Ruminococcus flavefaciens (Rf), Succiniclasticum (Su), and Prevotella (Pr) in the rumen was increased in the Astragalus group (p < 0.01), and metabolic profiling showed that the metabolites, such as L-lyrosine and L-leucine, were upregulated in the Astragalus group (p < 0.01). KEGG functional annotation revealed that upregulated metabolites were mainly enriched in the pathways of amino acid metabolism, lipid metabolism, fatty acid biosynthesis, and bile secretion in the Astragalus group, and downregulated metabolites were enriched in the pathways of methane metabolism and other pathways. Correlation analysis revealed that butyric acid was positively correlated with Roseburia and Blautia (p < 0.05) and negatively correlated with Desulfovibrio (p < 0.05). Thus, by analyzing the interactions of Astragalus root powder with the density of rumen microorganisms and their metabolites in lambs, it was shown that Astragalus root powder could improve the structure of rumen microbiota and their metabolites and then participate in the regulation of amino acid metabolism, lipid metabolism, immune metabolism, and other pathways to improve the efficiency of energy absorption of the lambs. Full article
(This article belongs to the Section Small Ruminants)
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<p>Determination of rumen microbiota density. <span class="html-italic">Bf</span>: <span class="html-italic">Butyrivibrio fibrisolvens</span>; <span class="html-italic">Cb</span>: <span class="html-italic">Clostridium butyricum</span>; <span class="html-italic">Sr</span>: <span class="html-italic">Selenomonas ruminantium</span>; <span class="html-italic">Fi</span>: <span class="html-italic">Fibrobacter</span>; <span class="html-italic">Pr</span>: <span class="html-italic">Prevotella</span>; <span class="html-italic">Rf</span>: <span class="html-italic">Ruminococcus flavefaciens</span>; <span class="html-italic">Tb</span>: <span class="html-italic">Treponema bryanti</span>; <span class="html-italic">Su</span>: <span class="html-italic">Succiniclasticum</span>. Note: ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Metabolome data quality control chart of rumen microbiota of lamb. (<b>A</b>) PCA; (<b>B</b>) OPLS-DA analysis. Note: biological replicates: n = 6.</p>
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<p>Differential metabolite analysis of lamb rumen microbiota metabolites. (<b>A</b>) Volcanic map of positive ion pattern differential metabolites; (<b>B</b>) negative map of positive ion pattern differential metabolites; (<b>C</b>) column chart of positive ion difference multiples; (<b>D</b>) column chart of negative ion difference multiples. Note: biological replicates: n = 6.</p>
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<p>KEGG function analysis of microbial differential metabolites (positive ion mode). (<b>A</b>) KEGG annotation of the classification diagram; (<b>B</b>) KEGG functional difference abundance score map. Note: biological replicates: n = 6.</p>
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<p>KEGG function analysis of microbial differential metabolites (negative ion mode). (<b>A</b>) KEGG annotation of the classification diagram; (<b>B</b>) KEGG functional difference abundance score map. Note: biological replicates: n = 6.</p>
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<p>Interaction analysis of rumen microbiome and metabolome. (<b>A</b>) Microbe–metabolite correlation heat map; (<b>B</b>) differential metabolite/differential microbiota correlation chord diagram; (<b>C</b>) heat map of correlation between fermentation microbiota and VFAs. ** means the difference is very significant, * means the difference is significant, no * means the difference is not significant. In the correlation chord diagram, a red string represents a positive correlation and a green string represents a negative correlation.</p>
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<p>Diagram of the mechanism of rumen microbiota–metabolite interactions. Text in red means upregulated in the <span class="html-italic">Astragalus</span> group, the text in blue means downregulated.</p>
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28 pages, 51497 KiB  
Review
Gecko-Inspired Controllable Adhesive: Structure, Fabrication, and Application
by Yanwei Liu, Hao Wang, Jiangchao Li, Pengyang Li and Shujuan Li
Biomimetics 2024, 9(3), 149; https://doi.org/10.3390/biomimetics9030149 - 1 Mar 2024
Cited by 2 | Viewed by 3873
Abstract
The gecko can achieve flexible climbing on various vertical walls and even ceilings, which is closely related to its unique foot adhesion system. In the past two decades, the mechanism of the gecko adhesion system has been studied in-depth, and a verity of [...] Read more.
The gecko can achieve flexible climbing on various vertical walls and even ceilings, which is closely related to its unique foot adhesion system. In the past two decades, the mechanism of the gecko adhesion system has been studied in-depth, and a verity of gecko-inspired adhesives have been proposed. In addition to its strong adhesion, its easy detachment is also the key to achieving efficient climbing locomotion for geckos. A similar controllable adhesion characteristic is also key to the research into artificial gecko-inspired adhesives. In this paper, the structures, fabrication methods, and applications of gecko-inspired controllable adhesives are summarized for future reference in adhesive development. Firstly, the controllable adhesion mechanism of geckos is introduced. Then, the control mechanism, adhesion performance, and preparation methods of gecko-inspired controllable adhesives are described. Subsequently, various successful applications of gecko-inspired controllable adhesives are presented. Finally, future challenges and opportunities to develop gecko-inspired controllable adhesive are presented. Full article
(This article belongs to the Section Biomimetics of Materials and Structures)
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Figure 1
<p>Gecko adhesive structures (reprinted with permission from Ref. [<a href="#B14-biomimetics-09-00149" class="html-bibr">14</a>]. Copyright 2006, Springer-Verlag). (<b>a</b>) The body of the gecko is usually in the centimeter range. (<b>b</b>) Lamellae structures on gecko paws, usually in the millimeter range. (<b>c</b>) Lamellae structures with micrometer-scale arrays of seta. (<b>d</b>) The ends of the seta have nanometer-scale spatulas.</p>
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<p>The process of exploring the sources of gecko adhesion.: suction [<a href="#B15-biomimetics-09-00149" class="html-bibr">15</a>]; electrostatic [<a href="#B26-biomimetics-09-00149" class="html-bibr">26</a>]; friction [<a href="#B16-biomimetics-09-00149" class="html-bibr">16</a>]; microinterlocking [<a href="#B17-biomimetics-09-00149" class="html-bibr">17</a>]; van der Waals (Autumn, K.) [<a href="#B19-biomimetics-09-00149" class="html-bibr">19</a>]; capillary force [<a href="#B22-biomimetics-09-00149" class="html-bibr">22</a>]; van der Waals (Pesika, N.S.) [<a href="#B25-biomimetics-09-00149" class="html-bibr">25</a>]; van der Waals (Puthoff, J.B.) [<a href="#B24-biomimetics-09-00149" class="html-bibr">24</a>]; electrostatic interactions [<a href="#B27-biomimetics-09-00149" class="html-bibr">27</a>]; acid-base interactions [<a href="#B29-biomimetics-09-00149" class="html-bibr">29</a>].</p>
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<p>Nanoscale spatula contacting the wall.</p>
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<p>Gecko controllable adhesion mechanism. (<b>a</b>) Microscopic adhesion mechanism [<a href="#B44-biomimetics-09-00149" class="html-bibr">44</a>]. (<b>b</b>) Macro motion of the foot [<a href="#B45-biomimetics-09-00149" class="html-bibr">45</a>]. (Refs. [<a href="#B44-biomimetics-09-00149" class="html-bibr">44</a>,<a href="#B45-biomimetics-09-00149" class="html-bibr">45</a>] were adapted through open access permission).</p>
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<p>Tilted micropillar array. (<b>a</b>) Tilted micropillars without controlled adhesion properties (reprinted with permission from Ref. [<a href="#B58-biomimetics-09-00149" class="html-bibr">58</a>]. Copyright 2007, American Chemical Society). (<b>b</b>) Directional polymer stalks (reprinted with permission from Ref. [<a href="#B59-biomimetics-09-00149" class="html-bibr">59</a>]. Copyright 2012, Taylor &amp; Francis). (<b>c</b>) Tilted high AR nanofibers (reprinted with permission from Ref. [<a href="#B60-biomimetics-09-00149" class="html-bibr">60</a>]. Copyright 2009, John Wiley and Sons). (<b>d</b>) Rigid polymer-polypropylene tilted microstructure arrays (reprinted with permission from Ref. [<a href="#B62-biomimetics-09-00149" class="html-bibr">62</a>]. Copyright 2008, American Institute of Physics). (<b>e</b>) Semi-cylindrical tilted microstructure (reprinted with permission from Ref. [<a href="#B63-biomimetics-09-00149" class="html-bibr">63</a>]. Copyright 2013, IOP Publishing Ltd).</p>
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<p>Diagram of wedge structure to realize a controllable adhesion force (vertical wedge structure as an example). The red part indicates the contact area between the adhesive and the wall.</p>
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<p>Wedge-shaped structural arrays. (<b>a</b>) Vertical wedge structures array (reprinted with permission from Ref. [<a href="#B64-biomimetics-09-00149" class="html-bibr">64</a>]. Copyright 2009, the Royal Society). (<b>b</b>) Array of circular wedge-shaped structures (reprinted with permission from Ref. [<a href="#B66-biomimetics-09-00149" class="html-bibr">66</a>]. Copyright 2017, John Wiley and Sons). (<b>c</b>) Array of wedge structures prepared on tungsten carbide molds (reprinted with permission from Ref. [<a href="#B68-biomimetics-09-00149" class="html-bibr">68</a>]. Copyright 2021, Tianfeng Zhou et al).</p>
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<p>Spatially variant microstructured adhesive with one-way friction (reprinted with permission from Ref. [<a href="#B71-biomimetics-09-00149" class="html-bibr">71</a>]. Copyright 2019, Srinivasan A. Suresh et al). (<b>a</b>) Definition of parameters for one-way adhesive geometry. (<b>b</b>) Application of a shear force in the preferred direction results in the flap deforming to conform to the surface, yielding a large contact area (blue). (<b>c</b>) The tallest wedge at the tip of the flap prevents any other wedge from contacting the surface, reducing the contact area (orange).</p>
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<p>Tip-modified adhesive. (<b>a</b>) Inclined micropillar structures with spherical and spade tips (reprinted with permission from Ref. [<a href="#B72-biomimetics-09-00149" class="html-bibr">72</a>]. Copyright 2012, Taylor &amp; Francis). (<b>b</b>) Nanoscale tilted microstructures with flat tips [<a href="#B73-biomimetics-09-00149" class="html-bibr">73</a>]. (<b>c</b>) Impregnation process modifies microstructures prepared by 3D printing (reprinted with permission from Ref. [<a href="#B74-biomimetics-09-00149" class="html-bibr">74</a>]. Copyright 2021, Springer Nature). (<b>d</b>) Tilted mushroom-shaped tip with modified impregnation process (reprinted with permission from Ref. [<a href="#B78-biomimetics-09-00149" class="html-bibr">78</a>]. Copyright 2009, John Wiley and Sons). (<b>e</b>) Tilted mushroom structure (reprinted with permission from Ref. [<a href="#B79-biomimetics-09-00149" class="html-bibr">79</a>]. Copyright 2014, American Chemical Society). (<b>f</b>) Rectangular cap tip structure (reprinted with permission from Ref. [<a href="#B80-biomimetics-09-00149" class="html-bibr">80</a>]. Copyright 2015, Yue Wang et al). (<b>g</b>) Inclined mushroom tip structure (reprinted with permission from Ref. [<a href="#B81-biomimetics-09-00149" class="html-bibr">81</a>]. Copyright 2020, Elsevier B.V.). (<b>h</b>) Stepped mushroom structure (reprinted with permission from Ref. [<a href="#B82-biomimetics-09-00149" class="html-bibr">82</a>]. Copyright 2016, American Chemical Society). (<b>i</b>) Mushroom-like structures containing TPS in the stem (reprinted with permission from Ref. [<a href="#B83-biomimetics-09-00149" class="html-bibr">83</a>]. Copyright 2023, Chohei Pang et al). (<b>j</b>) Inclined triangular prism with rectangular tip (reprinted with permission from Ref. [<a href="#B84-biomimetics-09-00149" class="html-bibr">84</a>]. Copyright 2013, John Wiley and Sons). (Ref. [<a href="#B73-biomimetics-09-00149" class="html-bibr">73</a>] was adapted through open access permission).</p>
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<p>Adhesives with SMP microstructures. (<b>a</b>) Adhesive prepared by Tecoflex 72D (reprinted with permission from Ref. [<a href="#B85-biomimetics-09-00149" class="html-bibr">85</a>]. Copyright 2007, John Wiley and Sons). (<b>b</b>) Pyramidal microstructures (reprinted with permission from Ref. [<a href="#B89-biomimetics-09-00149" class="html-bibr">89</a>]. Copyright 2013, American Chemical Society). (<b>c</b>) Micro-wedge array surface of a shape memory polymer (reprinted with permission from Ref. [<a href="#B90-biomimetics-09-00149" class="html-bibr">90</a>]. Copyright 2016, Elsevier Ltd).</p>
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<p>A schematic diagram of the working mechanism of an SMP underwater adhesive (reprinted with permission from Ref. [<a href="#B93-biomimetics-09-00149" class="html-bibr">93</a>]. Copyright 2018, John Wiley and Sons).</p>
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<p>Schematic representation of the adhesion mechanism of a controllable adhesive of shape memory polymers.</p>
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<p>Adhesives with magnetic microstructures. (<b>a</b>) Controllable adhesive with nickel beams (reprinted with permission from Ref. [<a href="#B94-biomimetics-09-00149" class="html-bibr">94</a>]. Copyright 2008, John Wiley and Sons). (<b>b</b>) Magnetically actuated arrays of micropillars (reprinted with permission from Ref. [<a href="#B95-biomimetics-09-00149" class="html-bibr">95</a>]. Copyright 2013, John Wiley and Sons). (<b>c</b>) Adhesives composed of lamellar structures and setal arrays (reprinted with permission from Ref. [<a href="#B96-biomimetics-09-00149" class="html-bibr">96</a>]. Copyright 2023, Springer Nature). (<b>d</b>) Slanted functional gradient micropillars (reprinted with permission from Ref. [<a href="#B97-biomimetics-09-00149" class="html-bibr">97</a>]. Copyright 2018, American Chemical Society).</p>
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<p>Adhesives with controllable back layers. (<b>a</b>) Adhesive with using embedded phase change material (reprinted with permission from Ref. [<a href="#B102-biomimetics-09-00149" class="html-bibr">102</a>]. Copyright 2010, IOP Publishing Ltd). (<b>b</b>) Hierarchal adhesive structure (reprinted with permission from Ref. [<a href="#B103-biomimetics-09-00149" class="html-bibr">103</a>]. Copyright 2020, American Chemical Society).</p>
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<p>Photolithography for the preparation of gecko-inspired controllable adhesives. (<b>a</b>) The photoresist is spin-coated on the substrate. (<b>b</b>) The photoresist is exposed with a mask from the front side. (<b>c</b>) The photoresist is precisely exposed by controlling the time. (<b>d</b>) The photoresist is precisely developed by controlling the time, leaving undercut holes. (<b>e</b>) Polymer is mixed, then poured on the mold and cured. (<b>f</b>) The cured polymer is demolded, leading to the cylindrical structure.</p>
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<p>Fabrication of gecko-inspired controllable adhesives. (<b>a</b>) Fabrication process of inclined micropillar fibers (reprinted with permission from Ref. [<a href="#B58-biomimetics-09-00149" class="html-bibr">58</a>]. Copyright 2007, American Chemical Society). (<b>b</b>) Two-step photolithographic fabrication process for step-shaped mushroom tip adhesive (reprinted with permission from Ref. [<a href="#B82-biomimetics-09-00149" class="html-bibr">82</a>]. Copyright 2016, American Chemical Society). (<b>c</b>) Ring wedge metal molds made by ultraprecision diamond cutting (reprinted with permission from Ref. [<a href="#B66-biomimetics-09-00149" class="html-bibr">66</a>]. Copyright 2017, John Wiley and Sons). (<b>d</b>) The schematic diagram of ultraprecision multistep and layered scribing (reprinted with permission from Ref. [<a href="#B109-biomimetics-09-00149" class="html-bibr">109</a>]. Copyright 2021, Springer Nature) (<b>e</b>) Two-photon lithography fabricates an adhesive with tilted mushroom-like tips (reprinted with permission from Ref. [<a href="#B81-biomimetics-09-00149" class="html-bibr">81</a>]. Copyright 2020, Elsevier B.V.). (<b>f</b>) Two-photon lithography to fabricate mushroom-like microstructures with TPS structures (reprinted with permission from Ref. [<a href="#B83-biomimetics-09-00149" class="html-bibr">83</a>]. Copyright 2023, Chohei Pang et al.).</p>
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<p>The climbing robots based on the gecko-inspired controllable adhesives. (<b>a</b>) Stickybot, a bioinspired robot capable of climbing smooth surfaces (reprinted with permission from Ref. [<a href="#B114-biomimetics-09-00149" class="html-bibr">114</a>]. Copyright 2008, IEEE).(<b>b</b>) Wall and ceiling climbing quadruped robot with superior water repellency (UNIclimb) (reprinted with permission from Ref. [<a href="#B118-biomimetics-09-00149" class="html-bibr">118</a>]. Copyright 2017, Springer Nature). (<b>c</b>) Gecko-inspired four-legged robot climbing on an inverted glass ceiling (reprinted with permission from Ref. [<a href="#B119-biomimetics-09-00149" class="html-bibr">119</a>]. Copyright 2021, Xiaosong LI et al.).</p>
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<p>Gecko grippers. (<b>a</b>) Shear force gripper holding a regulation-size basketball (reprinted with permission from Ref. [<a href="#B120-biomimetics-09-00149" class="html-bibr">120</a>]. Copyright 2015, IEEE). (<b>b</b>) An electrostatic/gecko-inspired adhesives soft robotic gripper (reprinted with permission from Ref. [<a href="#B124-biomimetics-09-00149" class="html-bibr">124</a>]. Copyright 2020, IEEE). (<b>c</b>) Gripper with three hybrid electrostatic/gecko adhesive (reprinted with permission from Ref. [<a href="#B125-biomimetics-09-00149" class="html-bibr">125</a>]. Copyright 2016, IEEE). (<b>d</b>) Mechanically flexible surface structures with embedded conductive electrodes grabbing oranges (reprinted with permission from Ref. [<a href="#B126-biomimetics-09-00149" class="html-bibr">126</a>]. Copyright 2023, Dong Geun KIM et al). (<b>e</b>) FarmHand demonstrates its gentle, hyperextended pinch on a raw egg, a high-force power grasp on a pumpkin (reprinted with permission from Ref. [<a href="#B127-biomimetics-09-00149" class="html-bibr">127</a>]. Copyright 2021, Wilson Ruotolo et al). (<b>f</b>) A cross-section of 3D assembly of the system from side and from bottom of the system. 1: silicone tubing, 2: vinylsiloxane, 3: outer case, 4: rubber ring, 5: soft chamber, 6: spacer between the chamber and the FAM, 7: FAM, and 8: mushroom-shaped PDMS microfiber [<a href="#B128-biomimetics-09-00149" class="html-bibr">128</a>]. (Ref. [<a href="#B128-biomimetics-09-00149" class="html-bibr">128</a>] was adapted through open access permission).</p>
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<p>Typical design of gecko-inspired controllable adhesive microstructures.</p>
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22 pages, 8411 KiB  
Article
Study of the Interactions between Muscle Fatty Acid Composition, Meat Quality-Related Genes and the Ileum Microbiota in Tibetan Sheep at Different Ages
by Fanxiong Wang, Yuzhu Sha, Xiu Liu, Yanyu He, Jiang Hu, Jiqing Wang, Shaobin Li, Pengyang Shao, Xiaowei Chen, Wenxin Yang, Qianling Chen, Min Gao and Wei Huang
Foods 2024, 13(5), 679; https://doi.org/10.3390/foods13050679 - 23 Feb 2024
Cited by 3 | Viewed by 1209
Abstract
The intestinal microbiota of ruminants is an important factor affecting animal production and health. Research on the association mechanism between the intestinal microbiota and meat quality of ruminants will play a positive role in understanding the formation mechanism of meat quality in ruminants [...] Read more.
The intestinal microbiota of ruminants is an important factor affecting animal production and health. Research on the association mechanism between the intestinal microbiota and meat quality of ruminants will play a positive role in understanding the formation mechanism of meat quality in ruminants and improving production efficiency. In this study, the fatty acid composition and content, expression of related genes, and structural characteristics of the ileum microbiota of ewes of Tibetan sheep at different ages (4 months, 1.5 years, 3.5 years, and 6 years) were detected and analyzed. The results revealed significant differences in fatty acid composition and content in the muscle of Tibetan sheep at different ages (p < 0.05); in addition, the content of MUFAs in the longissimus dorsi muscle and leg muscle was higher. Similarly, the expressions of muscle-related genes differed among the different age groups, and the expression of the LPL, SCD, and FABP4 genes was higher in the 1.5-year-old group. The ileum microbiota diversity was higher in the 1.5-year-old group, the Romboutsia abundance ratio was significantly higher in the 1.5-year-old group (p < 0.05), and there was a significant positive correlation with oleic acid (C18:1n9c) (p < 0.05). In conclusion, the content of beneficial fatty acids in the longissimus dorsi muscle and leg muscle of Tibetan sheep was higher at 1.5 years of age, and the best slaughter age was 1.5 years. This study provides a reference for in-depth research on the mechanism of the influence of the gut microbiota on meat quality and related regulation. Full article
(This article belongs to the Section Meat)
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<p>Expression analysis of genes related to dorsal longest muscle and leg muscle in Tibetan sheep of different ages. (<b>a</b>) Dorsal longest muscle gene expression analysis (<b>b</b>) Leg muscle gene expression analysis. Note: different lowercase letters indicate significant differences between ages at the <span class="html-italic">p</span> &lt; 0.05 level.</p>
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<p>Analysis of ileum microbiota diversity. (<b>a</b>) OTU Venn diagram analysis by age; (<b>b</b>) dilution curve analysis; (<b>c</b>) PCoA analysis; (<b>d</b>) Anosim analysis.</p>
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<p>Analysis of ileum microbiota diversity of different ages in Tibetan sheep. (<b>a</b>) Simpson; (<b>b</b>) Shannon; (<b>c</b>) ACE; (<b>d</b>) Chao1. Note: i4M represents the 4-month age group; i15Y represents the 1.5-year age group; i35Y represents the 3.5-year age group; and i6Y represents the 6-year age group. (* <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001). The same is below.</p>
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<p>Analysis of species composition. (<b>a</b>) Species composition at the phylum level; (<b>b</b>) Species composition at the genus level.</p>
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<p>LEFSe analysis.</p>
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<p>Figure functional prediction of the KEGG gene family. (<b>a</b>) 1.5-year-old age group and 4-month-old age group; (<b>b</b>) 1.5-year-old age group and 3.5-year-old age group; (<b>c</b>) 3.5-year-old age group and 6-year-old age group; (<b>d</b>) 4-month-old age group and 6-year-old age group.</p>
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<p>Functional prediction of the COG gene family. (<b>a</b>) 4-month-old age group and 6-year-old age group; (<b>b</b>) 1.5-year-old age group and 3.5-year-old age group.</p>
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<p>Correlation analysis of dorsal longest muscle and leg muscle of Tibetan sheep of different ages and their muscle fatty acids with related genes. (<b>a</b>) Heat map of the relationship between fatty acid content and composition in longissimus dorsi muscle and related genes in leg muscle. (<b>b</b>) Heat map of the relationship between fatty acid content and composition in leg muscle and related genes in leg muscle. Note: blue segments indicate negative correlation, red lines indicate positive correlation, solid lines indicate <span class="html-italic">p</span> &lt; 0.05, dashed lines indicate <span class="html-italic">p</span> ≥ 0.05.</p>
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<p>Microbiome-muscle fatty acids-muscle related gene correlation heat map. Note: * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Correlations between the ileum microbiota affecting muscle-related genes and regulating muscle fatty acid composition and content in Tibetan sheep of different ages. Note: black letters indicate upward adjustments, blue letters indicate downward adjustments, red arrows indicate positive correlations and blue arrows indicate negative correlations.</p>
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13 pages, 4556 KiB  
Article
Microstructure and Mechanical Properties of Refill Friction Stir Spot-Welded Joints of 2A12Al and 7B04Al: Effects of Tool Size and Welding Parameters
by Yisong Wang, Pengyang Li, Haitao Jiang, Kang Yang, Zhenhao Chen, Haijiao Chuai, Xiaoyan Wu, Qiang Meng and Lin Ma
Materials 2024, 17(3), 716; https://doi.org/10.3390/ma17030716 - 2 Feb 2024
Cited by 5 | Viewed by 1051
Abstract
To solve problems in dissimilarly light metal joints, refilled friction stir spot welding (RFSSW) is proposed instead of resistance spot welding. However, rotation speed, dwell time, plunge depth, and the diameter of welding tools all have a great influence on joints, which brings [...] Read more.
To solve problems in dissimilarly light metal joints, refilled friction stir spot welding (RFSSW) is proposed instead of resistance spot welding. However, rotation speed, dwell time, plunge depth, and the diameter of welding tools all have a great influence on joints, which brings great challenges in optimizing welding parameters to ensure their mechanical properties. In this study, the 1.5 mm thick 2A12Al and 2 mm thick 7B04Al lap joints were prepared by Taguchi orthogonal experiment design and RFSSW. The welding tool (shoulder) diameters were 5 mm and 7 mm, respectively. The macro/microstructures of the cross-section, the geometrical characteristics of the effective welding depth (EWD), the stir zone area (SZA), and the stir zone volume (SZV) were characterized. The shear strength and failure mode of the lap joint were analyzed using an optical microscope. It was found that EWD, SZA, and SZV had a good correlation with tensile–shear force. The optimal welding parameters of 5 mm diameter joints are 1500 rpm of rotation speed, 2.5 mm of plunge depth, and 0 s of dwell time, which for 7 mm joints are 1200 rpm, 1.5 mm, and 2 s. The tensile–shear force of 5 mm and 7 mm joints welded with these optical parameters was 4965 N and 5920 N, respectively. At the same time, the 5 mm diameter joints had better strength and strength stability. Full article
(This article belongs to the Collection Welding and Joining Processes of Materials)
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<p>Schematics of the (<b>a</b>) welding tools, (<b>b</b>) welding process, and (<b>c</b>) tensile shear test.</p>
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<p>Tensile–shear force of RFSSW joints for various welding parameters with diameters of (<b>a</b>) 5 mm and (<b>b</b>) 7 mm.</p>
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<p>Main benefits of factors affecting mechanical properties of welded joints with diameters of (<b>a</b>) 5 mm and (<b>b</b>) 7 mm.</p>
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<p>Cross-section morphologies of RFSSW joints under different parameters: (<b>a</b>–<b>c</b>) at the same RS of 900 rpm with different PDs and DTs; (<b>d</b>) at an RS of 1200 rpm, a PD of 2 mm, and a DT of 0 s; (<b>e</b>,<b>f</b>) at the same RS of 1500 rpm with different PDs and DTs.</p>
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<p>Macroscopic structures of the representative cross-section of joints with 7 mm diameter and 2 mm PD: (<b>a</b>) at an RS of 900 rpm and a DT of 1 s; (<b>b</b>) at an RS of 1200 rpm and a DT of 0 s; and (<b>c</b>) at an RS of 1500 rpm and a DT of 1 s.</p>
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<p>Morphologies of representative RFSSW joints under various welding parameters: (<b>a</b>,<b>b</b>) hole and end of effective binding in 5 mm 900-2.5-2 joint; (<b>c</b>,<b>d</b>) interfaces and end of effective binding in 5 mm 1500-2-2 joint; and (<b>e</b>,<b>f</b>) interface of SZ/TMAZ and adhesion ligaments in 7 mm 1200-2-0 joint.</p>
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<p>Plots of (<b>a</b>) effective welding depth (EWD), (<b>b</b>) stir zone area (SZA), and (<b>c</b>) stir zone volume (SZV) vs. tensile–shear force mean values for the representative Taguchi array welding condition.</p>
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<p>Typical cross-section macrograph of the representative 5 mm joint fractures: (<b>a</b>) 900-2.5-2, (<b>b</b>) 1200-2-0, and (<b>c</b>) 1500-2-2 (red circles and arrows are the points of crack initiation and the directions of crack propagation, respectively.).</p>
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<p>Typical cross-section macrograph of the representative 7 mm joint fractures: (<b>a</b>) 900-2.5-2, (<b>b</b>) 1200-2-0, and (<b>c</b>) 1500-1.5-1 (blue dotted lines and red arrows are the interfaces of alloys and the directions of crack propagation, respectively.).</p>
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21 pages, 8071 KiB  
Article
Study on Dynamic Characteristics of Pipeline Jet Cleaning Robot
by Hongwei Yan, Hailong Niu, Qi Chang, Pengyang Zhao and Bolong He
Actuators 2024, 13(2), 49; https://doi.org/10.3390/act13020049 - 26 Jan 2024
Cited by 2 | Viewed by 1766
Abstract
With the passage of time during pipeline operation, a substantial number of impurities accumulate and adhere to the inner wall of the pipeline. This deposition hinders the pipeline’s ability to function correctly, thereby posing significant hidden risks to people’s lives and the safety [...] Read more.
With the passage of time during pipeline operation, a substantial number of impurities accumulate and adhere to the inner wall of the pipeline. This deposition hinders the pipeline’s ability to function correctly, thereby posing significant hidden risks to people’s lives and the safety of their property. This article focuses on employing pipeline robots for internal cleaning. It examines the jet cleaning process of the spiral-driven pipeline inspection and cleaning robot, aiming to determine the optimal motion state and cleaning parameters for the device within the pipeline. The findings are verified and analyzed through experiments. It was observed that the cleaning effect is enhanced, with a target surface distance of approximately 12- to 13-times the diameter of the nozzle outlet (around 25 mm). In addition, an incident angle of 15° yields favorable cleaning results, with a maximum shear force exerted on the target surface of approximately 0.11 MPa. Ensuring that the pipelines operate reasonably and stably, thus guaranteeing their safe functioning and preventing significant economic and environmental damage, holds immense value. Full article
(This article belongs to the Section Actuators for Robotics)
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<p>Block diagram of the drive unit.</p>
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<p>Structure diagram of water jet cleaning unit.</p>
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<p>Structure of cleaning and collection unit.</p>
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<p>Structure of cleaning and collecting module.</p>
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<p>Patrol cleaning collection model.</p>
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<p>Flow model of jet nozzle.</p>
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<p>Jet cleaning model.</p>
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<p>Jet grid division diagram.</p>
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<p>Distribution of jet pressure 20 MPa, 30 MPa, 40 MPa, 50 MPa, 60 MPa target impact force.</p>
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<p>Jet shear force distribution diagram of jet pressure 20 MPa, 30 MPa, 40 MPa, 50 MPa, 60 Mpa.</p>
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<p>Target clearance model.</p>
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<p>Pressure change trend of target distance 10, 20, 30, and 40 mm. (<b>a</b>) The trend of pressure change with target distance; (<b>b</b>) The trend of speed change with target distance.</p>
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<p>Distribution of the hit pressure on the target surface.</p>
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<p>Wall shear stress distribution.</p>
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<p>Change in effective cleaning width of target surface under different target distances.</p>
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<p>Cleaning model of inclined target surface.</p>
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<p>Impact pressure curve at different incidence angles.</p>
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<p>Maximum shear force curve at different incident angles.</p>
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<p>Distribution of axial impact force on target surface with different jet angles.</p>
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<p>Cchange inof effective cleaning width of target surface at different jet angles.</p>
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<p>Process diagram of high-pressure water jet cleaning test.</p>
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<p>Ccomparison diagram of 30 mpa target impact force experiment and simulation.</p>
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21 pages, 7238 KiB  
Article
Research on Magnetic-Thermal-Force Multi-Physical Field Coupling of a High-Frequency Transformer with Different Winding Arrangements
by Bofan Li, Pengning Zhang, Pengyang Li, Ze Liu, Wei Li and Jian Zhang
Electronics 2023, 12(24), 5008; https://doi.org/10.3390/electronics12245008 - 14 Dec 2023
Cited by 2 | Viewed by 955
Abstract
In order to clarify the magnetic-thermal-force changing rule of high-frequency transformers under different winding arrangements, this paper tests the magnetization and loss characteristics of nanocrystalline materials at different temperatures, and based on the magnetization and loss data, establishes a magnetic-thermal-force coupling calculation model [...] Read more.
In order to clarify the magnetic-thermal-force changing rule of high-frequency transformers under different winding arrangements, this paper tests the magnetization and loss characteristics of nanocrystalline materials at different temperatures, and based on the magnetization and loss data, establishes a magnetic-thermal-force coupling calculation model of 15 kVA, 5 kHz nanocrystalline high-frequency transformers, and calculates and analyzes the magnetic flux density, loss and temperature rise distributions of high-frequency transformers with three different winding arrangements under no-load and short-circuit conditions, respectively. Through comparative analysis, it was found that under no-load conditions, the cross-transposition of winding has less influence on the magnetic flux of the high-frequency transformer core, but it can reduce the iron-core loss and transformer temperature rise. The cross-transposition of winding under short-circuit conditions can significantly reduce the leakage magnetic field strength of high-frequency transformers; complete cross-transposition weakens the high-frequency transformer losses and temperature rise better than partial cross-transposition. According to the winding current density and core leakage field distribution under short-circuit conditions, we calculated and analyzed the distribution of its the axial and radial electromagnetic forces. The results show that the axial electromagnetic force causes the winding to be squeezed from both ends to the middle, the radial electromagnetic force causes the primary winding to shrink inward and the secondary winding to expand outward, so cross-transposition can greatly reduce electromagnetic force and weakening the deformation of the winding. Therefore, high-frequency transformers of winding cross-transposed should be used in actual projects to reduce transformer temperature rise and improve efficiency and security. This research has theoretical significance for the multi-physical field coupling of high-frequency transformers and its structural design. Full article
(This article belongs to the Special Issue High Power Density Power Electronics)
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<p>Flow chat of electromagnetic field and temperature field coupled calculation of a high-frequency transformer.</p>
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<p>Schematic diagram of natural convection.</p>
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<p>Circuit-coupled magnetic field model.</p>
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<p>Simulation model of a high-frequency transformer.</p>
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<p>Schematic diagram of the core structure.</p>
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<p>Nanocrystalline measurement system.</p>
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<p>Magnetization curves of nanocrystalline core within the temperature range from 20 °C to 110 °C.</p>
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<p>Loss curves of nanocrystalline core within the temperature range from 20 °C to 110 °C.</p>
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<p>Schematics of the dual-active-bridge DC–DC converter.</p>
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<p>Non-sinusoidal voltage and current waveforms.</p>
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<p>Winding arrangement of high-frequency transformers.</p>
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<p>Distribution of magnetic density and loss fields of core under no-load conditions.</p>
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<p>Temperature of a high-frequency transformer under no-load conditions.</p>
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<p>Distribution of magnetic density and loss fields of windings under short-circuit conditions.</p>
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<p>Temperature of a high-frequency transformer under short-circuit conditions.</p>
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<p>Current density and leakage magnetic field intensity of windings under short-circuit conditions.</p>
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<p>Winding axial electromagnetic force.</p>
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<p>Winding radical electromagnetic force.</p>
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18 pages, 16167 KiB  
Article
Utilizing Grid Data and Deep Learning for Forest Fire Occurrences and Decision Support: A Case Study in the Ningxia Hui Autonomous Region
by Yakui Shao, Qin Zhu, Zhongke Feng, Linhao Sun, Peng Yue, Aiai Wang, Xiaoyuan Zhang and Zhiqiang Su
Forests 2023, 14(12), 2418; https://doi.org/10.3390/f14122418 - 12 Dec 2023
Cited by 1 | Viewed by 1279
Abstract
In order to investigate the geographical distribution of forest fire occurrences in the Ningxia Hui Autonomous Region, this study employs advanced modeling techniques, utilizing diverse data sources, including fuel, Gross Domestic Product (GDP), population, meteorology, buildings, and grid data. This study integrates deep [...] Read more.
In order to investigate the geographical distribution of forest fire occurrences in the Ningxia Hui Autonomous Region, this study employs advanced modeling techniques, utilizing diverse data sources, including fuel, Gross Domestic Product (GDP), population, meteorology, buildings, and grid data. This study integrates deep learning Convolutional Neural Networks (CNNs) to predict potential fire incidents. The research findings can be summarized as follows: (i) The employed model exhibits very good performance, achieving an accuracy of 84.35%, a recall of 86.21%, and an Area Under the Curve (AUC) of 87.67%. The application of this model significantly enhances the reliability of the forest fire occurrence model and provides a more precise assessment of its uncertainty. (ii) Spatial analysis shows that the risk of fire occurrence in most areas is low-medium, while high-risk areas are mainly concentrated in Longde County, Jingyuan County, Pengyang County, Xiji County, Yuanzhou District, Tongxin County, Xixia District, and Yinchuan City, which are mostly located in the southern, southeastern, and northwestern regions of Ningxia Hui Autonomous Region, with a total area of 2191.2 square kilometers. This underscores the urgent need to strengthen early warning systems and effective fire prevention and control strategies in these regions. The contributions of this research include the following: (i) The development of a highly accurate and practical provincial-level forest fire occurrence prediction framework based on grid data and deep learning CNN technology. (ii) The execution of a comprehensive forest fire prediction study in the Ningxia Hui Autonomous Region, China, incorporating multi-source data, providing valuable data references, and decision support for forest fire prevention and control. (iii) The initiation of a preliminary systematic investigation and zoning of forest fires in the Ningxia Hui Autonomous Region, along with tailored recommendations for prevention and control measures. Full article
(This article belongs to the Special Issue Integrated Measurements for Precision Forestry)
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<p>Location of study area.</p>
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<p>Ningxia’s topographic data comprises (<b>a</b>) elevation, (<b>b</b>) slope, and (<b>c</b>) aspect information.</p>
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<p>Ningxia weather station distribution map.</p>
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<p>Combustible load distribution (the combustible load refers to the combustible load in forested areas, measured in units of tons (t)).</p>
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<p>Map of socioeconomic conditions in Ningxia Autonomous Region (the POP is measured in “individuals”, the GDP is quantified in “thousands of yuan”, the count of buildings is in “units”, and the building area is assessed in “square meters”).</p>
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<p>Technical flow chart.</p>
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<p>Network Structure Diagram.</p>
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<p>The evaluation accuracy of the Convolutional Neural Network model (blue and green represent the training set and validation set, respectively).</p>
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<p>Probability and zoning map of forest fire risk in Ningxia Hui Autonomous Region (for probability and division classification, reference <a href="#forests-14-02418-t004" class="html-table">Table 4</a>).</p>
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34 pages, 35632 KiB  
Article
Spatial Prediction of Landslide Susceptibility Using Logistic Regression (LR), Functional Trees (FTs), and Random Subspace Functional Trees (RSFTs) for Pengyang County, China
by Hui Shang, Lixiang Su, Wei Chen, Paraskevas Tsangaratos, Ioanna Ilia, Sihang Liu, Shaobo Cui and Zhao Duan
Remote Sens. 2023, 15(20), 4952; https://doi.org/10.3390/rs15204952 - 13 Oct 2023
Cited by 7 | Viewed by 1769
Abstract
Landslides pose significant and serious geological threat disasters worldwide, threatening human lives and property; China is particularly susceptible to these disasters. This paper focuses on Pengyang County, which is situated in the Ningxia Hui Autonomous Region of China, an area prone to landslides. [...] Read more.
Landslides pose significant and serious geological threat disasters worldwide, threatening human lives and property; China is particularly susceptible to these disasters. This paper focuses on Pengyang County, which is situated in the Ningxia Hui Autonomous Region of China, an area prone to landslides. This study investigated the application of machine learning techniques for analyzing landslide susceptibility. To construct and validate the model, we initially compiled a landslide inventory comprising 972 historical landslides and an equivalent number of non-landslide sites (Data sourced from the Pengyang County Department of Natural Resources). To ensure an impartial evaluation, both the landslide and non-landslide datasets were randomly divided into two sets using a 70/30 ratio. Next, we extracted 15 landslide conditioning factors, including the slope angle, elevation, profile curvature, plan curvature, slope aspect, TWI (topographic wetness index), TPI (topographic position index), distance to roads and rivers, NDVI (normalized difference vegetation index), rainfall, land use, lithology, SPI (stream power index), and STI (sediment transport index), from the spatial database. Subsequently, a correlation analysis between the conditioning factors and landslide occurrences was conducted using the certainty factor (CF) method. Three landslide models were established by employing logistic regression (LR), functional trees (FTs), and random subspace functional trees (RSFTs) algorithms. The landslide susceptibility map was categorized into five levels: very low, low, medium, high, and very high susceptibility. Finally, the predictive capability of the three algorithms was assessed using the area under the receiver operating characteristic curve (AUC). The better the prediction, the higher the AUC value. The results indicate that all three models are predictive and practical, with only minor discrepancies in accuracy. The integrated model (RSFT) displayed the highest predictive performance, achieving an AUC value of 0.844 for the training dataset and 0.837 for the validation dataset. This was followed by the LR model (0.811 for the training dataset and 0.814 for the validation dataset) and the FT model (0.776 for the training dataset and 0.760 for the validation dataset). The proposed methods and resulting landslide susceptibility map can assist researchers and local authorities in making informed decisions for future geohazard prevention and mitigation. Furthermore, they will prove valuable and be useful for other regions with similar geological characteristics features. Full article
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<p>Location of the study area and landslide.</p>
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<p>Geomorphological map of Pengyang County.</p>
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<p>Drainage map of the study area.</p>
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<p>Flow chart of the study.</p>
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<p>Typical landslides at the research region: (<b>a</b>) landslide in Changgou Village, Honghe Township (106°40′47″E, 35°44′16″N); (<b>b</b>) landslide in Changgou Village, Honghe Township (106°47′51″E, 35°43′47″N); (<b>c</b>) landslide in Zhaike Village, Luowu Township (106°37′35″E, 35°10′05″N); (<b>d</b>) landslide in Zhaogou Village, Wangwa Township (106°41′47″E, 35°03′40″N).</p>
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<p>Landslide conditioning factors: (<b>a</b>) slope angle, (<b>b</b>) elevation, (<b>c</b>) profile curvature, (<b>d</b>) plan curvature, (<b>e</b>) slope aspect, (<b>f</b>) TWI, (<b>g</b>) TPI, (<b>h</b>) distance to roads, (<b>i</b>) distance to rivers, (<b>j</b>) NDVI, (<b>k</b>) rainfall, (<b>l</b>) land use, (<b>m</b>) lithology, (<b>n</b>) SPI, (<b>o</b>) STI.</p>
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<p>Landslide conditioning factors: (<b>a</b>) slope angle, (<b>b</b>) elevation, (<b>c</b>) profile curvature, (<b>d</b>) plan curvature, (<b>e</b>) slope aspect, (<b>f</b>) TWI, (<b>g</b>) TPI, (<b>h</b>) distance to roads, (<b>i</b>) distance to rivers, (<b>j</b>) NDVI, (<b>k</b>) rainfall, (<b>l</b>) land use, (<b>m</b>) lithology, (<b>n</b>) SPI, (<b>o</b>) STI.</p>
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<p>Landslide conditioning factors: (<b>a</b>) slope angle, (<b>b</b>) elevation, (<b>c</b>) profile curvature, (<b>d</b>) plan curvature, (<b>e</b>) slope aspect, (<b>f</b>) TWI, (<b>g</b>) TPI, (<b>h</b>) distance to roads, (<b>i</b>) distance to rivers, (<b>j</b>) NDVI, (<b>k</b>) rainfall, (<b>l</b>) land use, (<b>m</b>) lithology, (<b>n</b>) SPI, (<b>o</b>) STI.</p>
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<p>Landslide conditioning factors: (<b>a</b>) slope angle, (<b>b</b>) elevation, (<b>c</b>) profile curvature, (<b>d</b>) plan curvature, (<b>e</b>) slope aspect, (<b>f</b>) TWI, (<b>g</b>) TPI, (<b>h</b>) distance to roads, (<b>i</b>) distance to rivers, (<b>j</b>) NDVI, (<b>k</b>) rainfall, (<b>l</b>) land use, (<b>m</b>) lithology, (<b>n</b>) SPI, (<b>o</b>) STI.</p>
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<p>Histogram of the correlation of conditioning factors.</p>
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<p>LR model: (<b>a</b>) MSE value of training dataset; (<b>b</b>) MSE value of validation dataset.</p>
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<p>Landslide susceptibility maps: (<b>a</b>) LR model, (<b>b</b>) FT model, (<b>c</b>) RSFT model.</p>
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<p>Area percentages of landslide susceptibility classes.</p>
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<p>FT model (<b>a</b>) MSE value of training dataset; (<b>b</b>) MSE value of validation dataset.</p>
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<p>REST model: (<b>a</b>) MSE value of training dataset; (<b>b</b>) MSE value of validation dataset.</p>
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<p>ROC curves and prediction rate of three models on training dataset.</p>
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<p>ROC curves and prediction rate of the three models on the validation dataset.</p>
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<p>Histogram of the contribution of moderating factors: (<b>a</b>) CorrelationAttributeEval; (<b>b</b>) ReliefFAttributeEval; (<b>c</b>) GainRatioAttributeEval.</p>
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16 pages, 4236 KiB  
Article
Based on the Co-Evolution of lncRNAs-Microbiota and Metabolites in Rumen Epithelium to Analyze the Adaptation Characteristics of Tibetan Sheep to Nutrient Stress in the Cold Season
by Xiu Liu, Xinyu Guo, Yuzhu Sha, Yanyu He, Pengyang Shao, Jiang Hu, Jiqing Wang, Shaobin Li and Zhiyun Hao
Fermentation 2023, 9(10), 892; https://doi.org/10.3390/fermentation9100892 - 4 Oct 2023
Viewed by 1447
Abstract
Based on the serious phenomenon of Tibetan sheep “growing strong in warm seasons and losing weight in cold seasons”, this study explores the regulation of lncRNAs, microbiota, and metabolites in the cold season adaptation of Tibetan sheep from the perspective of the co-evolution [...] Read more.
Based on the serious phenomenon of Tibetan sheep “growing strong in warm seasons and losing weight in cold seasons”, this study explores the regulation of lncRNAs, microbiota, and metabolites in the cold season adaptation of Tibetan sheep from the perspective of the co-evolution of the host genome (first genome) and microbiome (second genome). RNA-seq results showed that 172 DE lncRNAs were identified in the rumen epithelium of Tibetan sheep in warm and cold seasons, of which 87 DE lncRNAs were significantly up-regulated in cold seasons. KEGG enrichment showed that target genes of up-regulated lncRNAs were significantly enriched in TNF signaling and oxidative phosphorylation pathways. LncRNA-mRNA regulatory network indicated that DE lncRNAs were involved in nutrient stress in the cold season by targeting ATP1B2, CADPS, TLR5, and UGT1A6. Correlation analysis showed some lncRNAs were significantly correlated with acetic acid, propionic acid, butyric acid, and rumen epithelial histomorphology and had a negative correlation with Butyrivibrio-2 and Succiniclasticum (p < 0.05). In addition, differential metabolites bilirubin and lncRNAs were co-enriched in the bile secretion pathway. lncRNAs played an important role in the adaptation process of Tibetan sheep in the cold season, and mediate the host to participate in nutrient absorption, energy utilization, and immune response, indicating that the host genome and microbial genome promote Tibetan sheep to adapt to nutrient stress in the cold season through co-evolution. Full article
(This article belongs to the Section Microbial Metabolism, Physiology & Genetics)
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<p>Identification and differential expression of lncRNAs. (<b>A</b>) Venn diagram of lncRNAs prediction; (<b>B</b>) statistical plot of lncRNAs; (<b>C</b>) volcano plot of differentially expressed lncRNAs; (<b>D</b>) clustering plot of differentially expressed lncRNAs.</p>
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<p>Analysis of GO enriched pathways.</p>
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<p>KEGG pathway analysis. (<b>A</b>) cis-target gene enrichment pathway; (<b>B</b>) trans-target gene enrichment pathway; (<b>C</b>) up-target gene enrichment pathway; (<b>D</b>) down-target gene enrichment pathway).</p>
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<p>lncRNA–mRNA targeting network diagram.</p>
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<p>Comparison of RT-qPCR and RNA-seq results.</p>
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<p>Correlation analysis of lncRNAs with VFAs and histological micromorphology. Note: * The correlation was significant at 0.05. A. indicated MSTRG.123203.4, B. indicated MSTRG.113717.2, C. indicated MSTRG.44204.2, D. indicated MSTRG.3973.1, E. indicated MSTRG.83755.1, F. indicated MSTRG.60784.1, G. indicated MSTRG.103129.28, H. indicated MSTRG.145005.2, I. indicated MSTRG.120061.1, J. indicated MSTRG.56302.1. MLT: Muscular layer thickness; NH: nipple height; NW: nipple width; SCT: Thickness of stratum corneum; SGT: stratum granulosum thickness; SST: stratum spinosum thickness; BLT: basal layer thickness.</p>
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<p>Analysis of interaction between lncRNAs and microbiota and metabolites. (<b>A</b>) Correlation heat map between LncRNA and microbiome; (<b>B</b>) LncRNA and metabolite enrichment pathway. Note: A. indicated MSTRG.123203.4, B. indicated MSTRG.113717.2, C. indicated MSTRG.44204.2, D. indicated MSTRG.3973.1, E. indicated MSTRG.83755.1, F. indicated MSTRG.60784.1, G. indicated MSTRG.103129.28, H. indicated MSTRG.145005.2, I. indicated MSTRG.120061.1, J. indicated MSTRG.56302.1. KEGG path maps are from the KEGG database and are licensed for copyright use. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Regulation model of differential lncRNAs on nutrient stress in the cold season.</p>
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19 pages, 4672 KiB  
Article
Interaction between Rumen Epithelial miRNAs-Microbiota-Metabolites in Response to Cold-Season Nutritional Stress in Tibetan Sheep
by Weibing Lv, Yuzhu Sha, Xiu Liu, Yanyu He, Jiang Hu, Jiqing Wang, Shaobin Li, Xinyu Guo, Pengyang Shao, Fangfang Zhao and Mingna Li
Int. J. Mol. Sci. 2023, 24(19), 14489; https://doi.org/10.3390/ijms241914489 - 23 Sep 2023
Viewed by 1681
Abstract
Tibetan sheep are already well adapted to cold season nutrient stress on the Tibetan Plateau. Rumen, an important nutrient for metabolism and as an absorption organ in ruminants, plays a vital role in the cold stress adaptations of Tibetan sheep. Ruminal microbiota also [...] Read more.
Tibetan sheep are already well adapted to cold season nutrient stress on the Tibetan Plateau. Rumen, an important nutrient for metabolism and as an absorption organ in ruminants, plays a vital role in the cold stress adaptations of Tibetan sheep. Ruminal microbiota also plays an indispensable role in rumen function. In this study, combined multiomics data were utilized to comprehensively analyze the interaction mechanism between rumen epithelial miRNAs and microbiota and their metabolites in Tibetan sheep under nutrient stress in the cold season. A total of 949 miRNAs were identified in the rumen epithelium of both cold and warm seasons. A total of 62 differentially expressed (DE) miRNAs were screened using FC > 1.5 and p value < 0.01, and a total of 20,206 targeted genes were predicted by DE miRNAs. KEGG enrichment analysis revealed that DE miRNA-targeted genes were mainly enriched in axon guidance(ko04360), tight junction(ko04530), inflammatory mediator regulation of TRP channels(ko04750) and metabolism-related pathways. Correlation analysis revealed that rumen microbiota, rumen VFAs and DE miRNAs were all correlated. Further study revealed that the targeted genes of cold and warm season rumen epithelial DE miRNAs were coenriched with differential metabolites of microbiota in glycerophospholipid metabolism (ko00564), apoptosis (ko04210), inflammatory mediator regulation of TRP channels (ko04750), small cell lung cancer (ko05222), and choline metabolism in cancer (ko05231) pathways. There are several interactions between Tibetan sheep rumen epithelial miRNAs, rumen microbiota, and microbial metabolites, mainly through maintaining rumen epithelial barrier function and host homeostasis of choline and cholesterol, improving host immunity, and promoting energy metabolism pathways, thus enabling Tibetan sheep to effectively respond to cold season nutrient stress. The results also suggest that rumen microbiota have coevolved with their hosts to improve the adaptive capacity of Tibetan sheep to cold season nutrient stress, providing a new perspective for the study of cold season nutritional stress adaptation in Tibetan sheep. Full article
(This article belongs to the Special Issue Molecular Genetics and Breeding Mechanisms in Domestics Animals)
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<p>Basic characterization of miRNA.</p>
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<p>(<b>A</b>) DE miRNAs volcano plot (Up: Significant upregulation of miRNAs in the cold season; Down: Significant downregulation of miRNAs in the cold season). (<b>B</b>) RT-qPCR validation of differentially expressed miRNAs.</p>
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<p>GO enrichment analysis. (<b>A</b>) Targeted genes for miRNAs that are significantly upregulated in the cold season. (<b>B</b>) Targeted genes for miRNAs that are significantly downregulated in the cold season.</p>
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<p>KEGG enrichment analysis. (<b>A</b>) Targeted genes for miRNAs that are significantly upregulated in the cold season. (<b>B</b>) Targeted genes for miRNAs that are significantly downregulated in the cold season.</p>
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<p>Correlation analysis between cold and warm season rumen epithelial DE miRNAs and microbiota. * Correlations differ at the 0.05 level; ** correlations differ at the 0.01 level. *** correlations differ at the 0.001 level. Same as below.</p>
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<p>Correlation analysis between cold and warm season rumen DE miRNAs and rumen VFAs. Note: The numbers in the figure represent the correlation coefficients between DE miRNAs and rumen VFAs. Red represents a positive correlation. Blue represents a negative correlation. The darker the color, the higher the correlation. * represents significant correlation between DE miRNAs and rumen VFAs; ** represents significant correlation between DE miRNAs and rumen VFAs.</p>
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<p>Correlation analysis between cold and warm season rumen epithelial DE miRNAs targeted genes and microbiota metabolites. Note: Red: cold upregulation. Green: cold downregulation. Blue: both upward and downward adjustments in the cold season. Circles: metabolites. Boxes: DE miRNA targeted genes. Rounded rectangles: signaling pathways. The direction of the arrow indicates the direction of the mode of action. The straight line represents direct action. The dotted line represents indirect action.</p>
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<p>The regulatory model of DE miRNAs in response to nutrient stress in the cold season. Note: The light color in the picture (<b>upper part</b>) indicates the space where the rumen contents exist. The dark color in the picture (<b>lower part</b>) indicates the rumen epithelial tissue. The arrow represents the direction of action. Red arrows represent promotion. Green arrows represent inhibition.</p>
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14 pages, 18057 KiB  
Article
Morphology and Distribution of Antennal Sensilla on Spodoptera frugiperda (Lepidoptera: Noctuidae) Larvae and Adults
by Wenwen Wang, Pengyang He, Tongxian Liu, Xiangfeng Jing and Shize Zhang
Diversity 2023, 15(9), 992; https://doi.org/10.3390/d15090992 - 4 Sep 2023
Cited by 2 | Viewed by 1680
Abstract
The invasive pest, Spodoptera frugiperda, commonly known as the fall armyworm (FAW), is a serious threat to food security in multiple countries worldwide. Insects’ antennal sensilla play a crucial role in perceiving plant odors and communication between male and female insects. This [...] Read more.
The invasive pest, Spodoptera frugiperda, commonly known as the fall armyworm (FAW), is a serious threat to food security in multiple countries worldwide. Insects’ antennal sensilla play a crucial role in perceiving plant odors and communication between male and female insects. This study aimed to examine the antennal morphology and sensilla variations on the antennae of FAW larvae and adults through scanning electron microscope analysis. The results revealed that third and fifth instar larval antennae possessed smell pores, sensilla pegs, and five types of antennal sensilla, namely sensilla trichodea, sensilla basiconica, sensilla chaetica, sensilla campaniform, and sensilla styloconicum, and the smell pores were first observed in Lepidoptera larvae. Furthermore, the size of sensilla in fifth instar larvae was significantly greater than those in third instar. On the adult antennae, there were smell pores and 12 types of sensilla identified: sensilla trichodea, sensilla basicaonica, sensilla auricillica, sensilla cavity, sensilla placodea, sensilla ligulate, Böhm’s bristles, sensilla chaetica, sensilla squamous, sensilla coeloconica, sensilla styloconicum, and sensilla uniporous peg. Notably, the sensilla cavity, sensilla placodea, sensilla ligulate, sensilla uniporous peg, and smell pores were first discovered in FAW adults. Compared with larvae, FAW adults have more types and amounts of sensilla. Additionally, we also discussed the possible functions of these antennal sensilla. This study provides valuable information for a comprehensive understanding of the type and function of antennal sensilla in FAW and assists in the development of novel pest control strategies, such as pest behavior control technology, for the prevention of this invasive pest. Full article
(This article belongs to the Topic Arthropod Biodiversity: Ecological and Functional Aspects)
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<p>The antennal morphological characteristics of <span class="html-italic">Spodoptera frugiperda</span> larvae. (<b>A</b>) Scape (S), pedicel (P), and flagellum (F) of 3rd-instar larvae; (<b>B</b>) Pedicel (P) and flagellum (F) of 5th-instar larvae.</p>
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<p>The sensilla, smell pores, and sensilla pegs of <span class="html-italic">Spodoptera frugiperda</span> larvae. (<b>A</b>) Sensilla on the pedicel; (<b>B</b>) Sensilla on the flagellum; (<b>C</b>) Sensilla trichodea, sensilla basiconica I, and sensilla campaniform; (<b>D</b>) Sensilla chaetica, sensilla basiconica I and II; (<b>E</b>) Sensilla chaetica, sensilla styloconicum, sensilla basiconica I, and smell pores; (<b>F</b>) Sensilla basiconica I and sensilla campaniform. ST I: Sensilla trichodea I; ST II: Sensilla trichodea II; SB I: Sensilla basiconica I; SB II: Sensilla basiconica II; SCam: Sensilla campaniform; SSt: Sensilla styloconicum; SCh: Sensilla chaetica; SP: Smell pores; F: Flagellum.</p>
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<p>The antennae morphological characteristics of <span class="html-italic">Spodoptera frugiperda</span> adults. (<b>A</b>) Overall appearance of adult antennae; (<b>B</b>) Scape, pedicel, and flagellum; (<b>C</b>) Dorsal side of the flagellum; (<b>D</b>) Ventral side of the flagellum; (<b>E</b>) The end of the flagellum; (<b>F</b>) The tip of the flagellum. ♀: Female; ♂: Male; S: Scape; P: Pedicel; F: Flagellum.</p>
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<p>The sensilla morphology of <span class="html-italic">Spodoptera frugiperda</span> adults. (<b>A</b>) The distribution of Böhm bristles; (<b>B</b>) Böhm’s bristles; (<b>C</b>) Sensilla trichodea; (<b>D</b>) The tip of sensilla trichodea; (<b>E</b>) The thick wall of sensilla trichodea; (<b>F</b>) Sensilla basiconica; (<b>G</b>) Sensilla chaetica; (<b>H</b>) Sensilla chaetica and sensilla squamous on the dorsal flagellum; (<b>I</b>) Sensilla coeloconica. BB: Böhm’s bristles; BB I: Böhm’s bristles I; BB II: Böhm’s bristles II; ST: Sensilla trichodea; SB: Sensilla basiconica; SCh: Sensilla chaetica; SCo: Sensilla coeloconica; SSq: Sensilla squamous.</p>
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<p>The sensilla and smell pores morphology of <span class="html-italic">Spodoptera frugiperda</span> adults. (<b>A</b>) Sensilla on the dorsal flagellum; (<b>B</b>,<b>C</b>) Sensilla styloconicum; (<b>D</b>) Sensilla cavity; (<b>E</b>) Sensilla squamous and smell pores; (<b>F</b>) Sensilla auricillica; (<b>G</b>) Sensilla ligulate; (<b>H</b>) Sensilla uniporous peg; (<b>I</b>) Sensilla placodea. SSt: Sensilla styloconicum; SSq: Sensilla squamous; SA: Sensilla auricillica; SL: Sensilla ligulate; SU: Sensilla uniporous peg; SPl: Sensilla placodea; SP: Smell pores; SCo: Sensilla coeloconica; ST: Sensilla trichodea; SCh: Sensilla chaetica; SCa: Sensilla cavity.</p>
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23 pages, 7106 KiB  
Article
Identification of Ecological Restoration Approaches and Effects Based on the OO-CCDC Algorithm in an Ecologically Fragile Region
by Caiyong Wei, Xiaojing Xue, Lingwen Tian, Qin Yang, Bowen Hou, Wenlong Wang, Dawei Ma, Yuanyuan Meng and Xiangnan Liu
Remote Sens. 2023, 15(16), 4023; https://doi.org/10.3390/rs15164023 - 14 Aug 2023
Cited by 1 | Viewed by 1386
Abstract
A full understanding of the patterns, trends, and strategies for long-term ecosystem changes helps decision-makers evaluate the effectiveness of ecological restoration projects. This study identified the ecological restoration approaches on planted forest, natural forest, and natural grassland protection during 2000–2022 based on a [...] Read more.
A full understanding of the patterns, trends, and strategies for long-term ecosystem changes helps decision-makers evaluate the effectiveness of ecological restoration projects. This study identified the ecological restoration approaches on planted forest, natural forest, and natural grassland protection during 2000–2022 based on a developed object-oriented continuous change detection and classification (OO-CCDC) method. Taking the Loess hilly region in the southern Ningxia Hui Autonomous Region, China as a case study, we assessed the ecological effects after protecting forest or grassland automatically and continuously by highlighting the location and change time of positive or negative effects. The results showed that the accuracy of ecological restoration approaches extraction was 90.73%, and the accuracies of the ecological restoration effects were 86.1% in time and 84.4% in space. A detailed evaluation from 2000 to 2022 demonstrated that positive effects peaked in 2013 (1262.69 km2), while the highest negative effects were observed in 2017 (54.54 km2). In total, 94.39% of the planted forests, 99.56% of the natural forest protection, and 62.36% of the grassland protection were in a stable pattern, and 35.37% of the natural grassland displayed positive effects, indicating a proactive role for forest management and ecological restoration in an ecologically fragile region. The negative effects accounted for a small proportion, only 2.41% of the planted forests concentrated in Pengyang County and 2.62% of the natural grassland protection mainly distributed around the farmland in the central-eastern part of the study area. By highlighting regions with positive effects as acceptable references and regions with negative effects as essential conservation objects, this study provides valuable insights for evaluating the effectiveness of the integrated ecological restoration pattern and determining the configuration of ecological restoration measures. Full article
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<p>Study area: (<b>a</b>) general location in China; (<b>b</b>) location within Ningxia; and (<b>c</b>) digital elevation model (DEM).</p>
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<p>Workflow of restoration effects identification of ecological restoration approaches based on the proposed OO-CCDC.</p>
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<p>The number of Landsat images from 2000 to 2022.</p>
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<p>The distribution of sampling points.</p>
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<p>(<b>a</b>) Three ecological restoration approaches of Landsat imagery cutouts during 2000–2022 and photos taken in the field: site 1, site 2, and site 3 represent natural forest protection, planted forest, and natural grass protection, respectively. (<b>b</b>) NDVI time series at the object level of the three ecological restoration approaches. (<b>c</b>) EVI time series at the object level of the three ecological restoration approaches.</p>
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<p>The ecological restoration effects of (<b>a</b>) natural forest protection, (<b>b</b>) planted forest, and (<b>c</b>) natural grass protection.</p>
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<p>Error distribution of detection time.</p>
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<p>Comparison of identification results by two algorithms in five typical regions. Blue boundary represents the detection results by OO-CCDC, while red boundary represents the detection results by CCDC.</p>
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<p>(<b>a</b>) The distribution of ecological restoration approaches in 2022, and (<b>b</b>) the area of each approach.</p>
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<p>The distribution of (<b>a</b>) recovered, (<b>b</b>) degraded, and (<b>c</b>) stable areas, and (<b>d</b>) the statistics of the three ecological restoration approaches.</p>
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<p>Distribution of natural forest protection, planted forest, and natural grass protection of different restoration effects, and recovery/degradation year. Some regions framed in red are enlarged to show more details.</p>
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<p>Years of different ecological restoration approaches recovery and degradation.</p>
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<p>ROC-LV of different Scale.</p>
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